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Real-World Use of Hybrid Closed-Loop Systems during Diabetes Camp: A Preliminary Study for Secure Configuration
María José Olid-Cárdenas1,2,3, Alfonso Lendínez-Jurado3,4,5, Gabriela Monroy-Rodríguez6,7
1Department of Marketing and Communication, Faculty of Communication, European University of Madrid, 28670 Villaviciosa de Odón, Spain.
Insights
Closed-loop systems effectively manage pediatric type 1 diabetes during summer camp, maintaining target glucose levels without increasing hypoglycemia or ketoacidosis risks, even with routine deviations.
Area of Science:
- Pediatric Endocrinology
- Diabetes Technology
- Metabolic Disease Management
Background:
- Closed-loop systems have transformed pediatric diabetes care.
- Limited data exists on system performance during non-routine activities like summer camp.
Purpose of the Study:
- To evaluate the safety and efficacy of closed-loop systems in pediatric type 1 diabetes patients during a summer camp.
- To assess glucose control and system functionality during deviations from normal routines.
Main Methods:
- A prospective, single-center preliminary study.
- 27 pediatric type 1 diabetes patients (Medtronic MiniMed 780G and Tandem Control-IQ) were monitored during a 7-day camp and 3 weeks post-camp.
- Key metrics included Time in Range (TIR), Time Below Range (TBR), and Time Above Range (TAR).
Main Results:
- Target TIR of 70% was consistently met.
- Worst TBR occurred at 72 hours; worst TAR in the first 24 hours, with subsequent improvement.
- No severe hypoglycemia (Level 3) or diabetic ketoacidosis episodes were reported.
Conclusions:
- Specific programming in closed-loop systems is safe for pediatric type 1 diabetes patients during summer camp.
- These systems effectively manage glucose levels despite increased physical activity and altered feeding routines.
- No increased risk of severe hypoglycemia or ketoacidosis was observed, regardless of the device used.
Abstract:
The introduction of closed-loop systems in the pediatric population has been a revolution in the management and evolution of diabetes. However, there are not many published studies in situations in which the feeding, schedules, and activities of the children deviate from the routine for which the systems were programmed, as in the case of a summer camp for children and adolescents with diabetes, where the specific programming of this device is not well known. It was a single-center prospective preliminary study. A total of twenty-seven patients (mean age 11.9 ± 1.9 years, 40% male, duration of diabetes 6.44 ± 2.83 years) were included (twenty with Medtronic MiniMed 780G system and seven with Tandem Control-IQ). Glucometric variables and pump functionality were monitored during the 7-day camp and in the following 3 weeks. There was no decrease from the objective TIR 70% at any moment. The worst results in Time Below Range were at 72 h from starting the camp, and the worst results in Time Above Range were in the first 24 h, with a progressive improvement after that. No episodes of level 3 hypoglycemia or ketoacidosis occurred. The use of specific programming in two integrated systems, with complex blood glucose regulation algorithms and not-prepared-for situations with increased levels of physical activity or abrupt changes in feeding routines, did not result in an increased risk of level 3 hypoglycemia and ketoacidosis for our pediatric type 1 diabetes (T1D) patients, regardless of the closed-loop device.
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